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	<title>Pulmonary Fibrosis News Forums | Margaret | Activity</title>
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				<title>Margaret replied to the discussion Do you suffer from fever often? in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/do-you-suffer-from-fever-often/#post-37184</link>
				<pubDate>Mon, 17 Jun 2024 07:30:07 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/do-you-suffer-from-fever-often/#post-37184"><span class="bb-reply-lable">Reply to</span> Do you suffer from fever often?</a></p> <div class="bb-content-inr-wrap"><p>Not all types of pulmonary fibrosis are the same. Low grade fever is a symptom of RIPF along with SOB and dropping oxygen levels. As often happens in this situation I was unsuccessfully treated with antibiotics for several months until a CT was done and my radiation oncologist was brought into the loop. Delaying corticosteroids meant most of&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-42574"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/do-you-suffer-from-fever-often/#post-37184" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Breathlessness at the dentist in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/breathlessness-at-the-dentist/#post-37109</link>
				<pubDate>Wed, 29 May 2024 05:15:40 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/breathlessness-at-the-dentist/#post-37109"><span class="bb-reply-lable">Reply to</span> Breathlessness at the dentist</a></p> <div class="bb-content-inr-wrap"><p>I have problems with coughing. My steroid inhaler generally works pretty well but an open mouth means air reaches exposed nerves and triggers coughing. My dentist keeps me at the office for a longer time and works on my mouth in short intervals. She sees other patients when I am having breaks. I end up spending a morning at the dentist rather&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-42437"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/breathlessness-at-the-dentist/#post-37109" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Prednisone Reduction and low oxygen in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/prednisone-reduction-and-low-oxygen/#post-36718</link>
				<pubDate>Mon, 04 Mar 2024 02:57:32 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/prednisone-reduction-and-low-oxygen/#post-36718"><span class="bb-reply-lable">Reply to</span> Prednisone Reduction and low oxygen</a></p> <div class="bb-content-inr-wrap"><p>While my PF has a different cause (radiation induced) I take prednisone to reduce inflammation and help with the cough. It does have side effects but there are ways to reduce them. I take alendronate for bone loss (there are other meds for this as well) and eat a low carb diet to prevent blood sugar issues. If prednisone is helping your&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-41775"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/prednisone-reduction-and-low-oxygen/#post-36718" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Do you suffer from fever often? in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/do-you-suffer-from-fever-often/#post-36624</link>
				<pubDate>Sat, 17 Feb 2024 07:53:28 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/do-you-suffer-from-fever-often/#post-36624"><span class="bb-reply-lable">Reply to</span> Do you suffer from fever often?</a></p> <div class="bb-content-inr-wrap"><p>I had low grade fevers along with SOB and severe dry cough when I was diagnosed with radiation induced PF from breast cancer treatment. The scarring pattern is different from IPF and imaging over time showed it spreading out from the radiation field. I take prednisone for the RIPF and no longer have a fever unless I’m ill with something else.&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-41603"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/do-you-suffer-from-fever-often/#post-36624" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion IPF Cough vs Bronchitis Cough in the forum Using Our Forums</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-cough-vs-bronchitis-cough/#post-36225</link>
				<pubDate>Mon, 27 Nov 2023 04:52:54 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-cough-vs-bronchitis-cough/#post-36225"><span class="bb-reply-lable">Reply to</span> IPF Cough vs Bronchitis Cough</a></p> <div class="bb-content-inr-wrap"><p>I have a severe dry cough originating deep in my lungs from PF (radiation induced) that would cause me to pass out momentarily from a large drop in oxygen. It happened during a PFT when that was seen on the monitor. The cough is now pretty well controlled by Flovent.</p>
<p>I have had both bronchitis with a wet cough higher up and pneumonia with a&hellip;</p>
<p><span class="activity-read-more" id="activity-read-more-40877"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/ipf-cough-vs-bronchitis-cough/#post-36225" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Antibiotics adversely affecting IPF in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/antibiotics-adversely-affecting-ipf/#post-36051</link>
				<pubDate>Tue, 17 Oct 2023 03:55:31 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/antibiotics-adversely-affecting-ipf/#post-36051"><span class="bb-reply-lable">Reply to</span> Antibiotics adversely affecting IPF</a></p> <div class="bb-content-inr-wrap"><p>There is a website pneumotox.com where you can enter the generic name of a drug and see any pulmonary interactions. Those with an ILD side effect listed should be investigated. The statin I take is not my PCP’s first choice for that reason.</p>
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				<title>Margaret replied to the discussion Tests interval in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/tests-interval/#post-34864</link>
				<pubDate>Tue, 11 Apr 2023 13:10:56 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tests-interval/#post-34864"><span class="bb-reply-lable">Reply to</span> Tests interval</a></p> <div class="bb-content-inr-wrap"><p>Dr. Strum &#8211; Thank you for your reply. I have a math/science background and am comfortable reading scientific papers even though I occasionally have to look up the definition of a medical term. While limited lung fibrosis from radiation is not unheard of the progressive &#8220;recall&#8221; RIPF is rare (for breast cancer 3/1000 radiation patients.)&hellip;<span class="activity-read-more" id="activity-read-more-38275"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tests-interval/#post-34864" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Tests interval in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/tests-interval/#post-34861</link>
				<pubDate>Mon, 10 Apr 2023 07:21:13 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tests-interval/#post-34861"><span class="bb-reply-lable">Reply to</span> Tests interval</a></p> <div class="bb-content-inr-wrap"><p>CTs are done more frequently if there is a reason they are needed. My doctor is monitoring several slowly growing pulmonary nodules so a CT is done every 3 to 6 months. My last one showed returning infiltrates before I had any worsening symptoms so I went back on oral prednisone for a while.</p>
<p>Mary Frances &#8211; My PF is radiation induced&hellip;<span class="activity-read-more" id="activity-read-more-38258"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/tests-interval/#post-34861" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Shortness of breath and how to catch it in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/shortness-of-breath-and-how-to-catch-it/#post-34852</link>
				<pubDate>Sat, 08 Apr 2023 00:48:00 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/shortness-of-breath-and-how-to-catch-it/#post-34852"><span class="bb-reply-lable">Reply to</span> Shortness of breath and how to catch it</a></p> <div class="bb-content-inr-wrap"><p>Arthur, Talking causes SOB and coughing for me. I had to retire from teaching because of it. My O2 levels are in the low 90s. Inhaled corticosteroids and gabapentin help with the coughing. I try to remember to pause between sentences when talking.</p>
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				<title>Margaret replied to the discussion How to Decide When to Stop Working with Pulmonary Fibrosis. in the forum Employment &#38; Pulmonary Fibrosis</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/decide-stop-working-pulmonary-fibrosis/#post-34789</link>
				<pubDate>Wed, 29 Mar 2023 06:10:23 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/decide-stop-working-pulmonary-fibrosis/#post-34789"><span class="bb-reply-lable">Reply to</span> How to Decide When to Stop Working with Pulmonary Fibrosis.</a></p> <div class="bb-content-inr-wrap"><p>I too loved my teaching job but had to retire at the end of the 2022 school year after being diagnosed with PF (radiation induced) five months earlier. The talking required caused SOB and frequent severe coughing. I still miss working terribly but I had no choice since I developed cough syncope (briefly passing out caused by the violent&hellip;<span class="activity-read-more" id="activity-read-more-38105"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/decide-stop-working-pulmonary-fibrosis/#post-34789" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Symptoms vs O2 levels in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/symptoms-vs-o2-levels/#post-34653</link>
				<pubDate>Fri, 17 Mar 2023 00:16:27 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/symptoms-vs-o2-levels/#post-34653"><span class="bb-reply-lable">Reply to</span> Symptoms vs O2 levels</a></p> <div class="bb-content-inr-wrap"><p>O2 levels can change in an instant. During my last PFT a coughing fit caused me to pass out. My levels are generally in the low 90s but dropped to 40 on the monitor and recovered in about 15 seconds according to the tech. I thought my cough was fairly well controlled (25 episodes a day rather than the prior 125) but my pulmonologist increased&hellip;<span class="activity-read-more" id="activity-read-more-37884"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/symptoms-vs-o2-levels/#post-34653" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Prednisone/Vitamin D deficiency in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/prednisone-vitamin-d-deficiency/#post-34600</link>
				<pubDate>Sat, 11 Mar 2023 05:08:56 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/prednisone-vitamin-d-deficiency/#post-34600"><span class="bb-reply-lable">Reply to</span> Prednisone/Vitamin D deficiency</a></p> <div class="bb-content-inr-wrap"><p>Prednisone and inhaled corticosteroids really help my inflammation and my cough. I was taking 2000 iu vitamin D daily but my blood levels were low so I now take 4000 iu daily. If you don’t know what your level is you can ask your doctor for a blood test to check.</p>
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				<title>Margaret replied to the discussion cooking fumes in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/cooking-fumes/#post-34497</link>
				<pubDate>Sun, 26 Feb 2023 04:47:37 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/cooking-fumes/#post-34497"><span class="bb-reply-lable">Reply to</span> cooking fumes</a></p> <div class="bb-content-inr-wrap"><p>Cooking fumes are harmful to the lungs. When I was younger I worked in a commercial kitchen where the fumes were much worse than in a home kitchen. I have a good range hood and open a nearby window no matter what the weather to help cut down on the indoor pollution.</p>
<p>Wearing a respirator mask can help but it impedes my breathing too much.</p>
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				<title>Margaret replied to the discussion Lung Biopsy in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/lung-biopsy/#post-34384</link>
				<pubDate>Sat, 11 Feb 2023 03:49:59 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/lung-biopsy/#post-34384"><span class="bb-reply-lable">Reply to</span> Lung Biopsy</a></p> <div class="bb-content-inr-wrap"><p>Is the biopsy being done to see if you would be eligible for a lung transplant? If so, the risks might be worth it for you. My pulmonologist told me he  recommends biopsies only if they will be used to determine treatment because of the risk involved. Good luck with your decision.</p>
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				<title>Margaret replied to the discussion Prednisone in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/prednisone/#post-33958</link>
				<pubDate>Fri, 23 Dec 2022 01:46:42 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/prednisone/#post-33958"><span class="bb-reply-lable">Reply to</span> Prednisone</a></p> <div class="bb-content-inr-wrap"><p>After several months on high dose prednisone my pulmonologist tapered me down to a corticosteroid inhaler (Flovent HFA.) It targets the lungs so the bad systemic side effects (high blood sugar, bone thinning, insomnia) are eliminated and the SOB and cough remain improved.</p>
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				<title>Margaret replied to the discussion Medication Storage &#38; Transport in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/medication-storage-transport/#post-33957</link>
				<pubDate>Fri, 23 Dec 2022 01:28:25 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/medication-storage-transport/#post-33957"><span class="bb-reply-lable">Reply to</span> Medication Storage & Transport</a></p> <div class="bb-content-inr-wrap"><p>Lunch bags and small coolers come in a variety of shapes, sizes and styles. They have handles or straps for carrying and are easy to clean. Some have a variety of compartments to separate equipment like a nebulizer from prescription bottles. It’s amazing how the medications seem to multiply but I’m glad to have them.</p>
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				<title>Margaret replied to the discussion Saw PF on xray now what in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/saw-pf-on-xray-now-what/#post-33860</link>
				<pubDate>Wed, 14 Dec 2022 08:41:18 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/saw-pf-on-xray-now-what/#post-33860"><span class="bb-reply-lable">Reply to</span> Saw PF on xray now what</a></p> <div class="bb-content-inr-wrap"><p>Hi Chris, RIPF is radiation induced pulmonary fibrosis (a side effect of radiation therapy to the chest for cancer.) There are over 200 types of interstitial lung disease and consequently lots of acronyms and a variety of treatments. You would have to check with your doctor to see if those drugs were a problem in your case. My pulmonologist&hellip;<span class="activity-read-more" id="activity-read-more-36505"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/saw-pf-on-xray-now-what/#post-33860" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Saw PF on xray now what in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/saw-pf-on-xray-now-what/#post-33846</link>
				<pubDate>Tue, 13 Dec 2022 17:33:40 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/saw-pf-on-xray-now-what/#post-33846"><span class="bb-reply-lable">Reply to</span> Saw PF on xray now what</a></p> <div class="bb-content-inr-wrap"><p>Everybody needs to make vax decisions based on their own situation.  I have had every vaccine going because any respiratory infection, even a cold, could start the RIPF progression again. I also have to avoid about 300 medications and intubation (like for surgery) since they are progression triggers in RIPF, too. I&#8217;m still living the&hellip;<span class="activity-read-more" id="activity-read-more-36468"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/saw-pf-on-xray-now-what/#post-33846" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Saw PF on xray now what in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/saw-pf-on-xray-now-what/#post-33842</link>
				<pubDate>Tue, 13 Dec 2022 06:47:00 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/saw-pf-on-xray-now-what/#post-33842"><span class="bb-reply-lable">Reply to</span> Saw PF on xray now what</a></p> <div class="bb-content-inr-wrap"><p>Hi Chris,</p>
<p>Given the history of mold and dust exposure it could be Hypersensitivity Pneumonitis. HP can be acute or progressive. Removing the irritant can stop the progression which might explain the small amount of fibrosis. Corticosteroids can also help.</p>
<p>I have radiation induced pulmonary fibrosis caused by breast cancer treatment. While&hellip;<span class="activity-read-more" id="activity-read-more-36463"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/saw-pf-on-xray-now-what/#post-33842" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion C-PET Scan in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/c-pet-scan/#post-33686</link>
				<pubDate>Thu, 24 Nov 2022 19:26:28 -0600</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/c-pet-scan/#post-33686"><span class="bb-reply-lable">Reply to</span> C-PET Scan</a></p> <div class="bb-content-inr-wrap"><p>Hi Charlene, I have radiation induced pulmonary fibrosis rather than IPF (different scarring pattern and often responsive to corticosteroids) and I was doing a PFT (not a C-PET), but the tech inadvertently managed to provoke severe breathlessness, hypoxia and coughing by noticing that I was only using my good left lung and favoring my bad&hellip;<span class="activity-read-more" id="activity-read-more-36203"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/c-pet-scan/#post-33686" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion all us old folks with radiation induced pulmonary fibrosis???? in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/all-us-old-folks-with-radiation-induced-pulmonary-fibrosis/#post-33011</link>
				<pubDate>Fri, 02 Sep 2022 17:17:54 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/all-us-old-folks-with-radiation-induced-pulmonary-fibrosis/#post-33011"><span class="bb-reply-lable">Reply to</span> all us old folks with radiation induced pulmonary fibrosis????</a></p> <div class="bb-content-inr-wrap"><p>Thank you for the information, Anna.  It&#8217;s good to see that someone is discussing ILDs other than IPF even though they are less common.</p>
<p>Margaret</p>
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				<title>Margaret replied to the discussion all us old folks with radiation induced pulmonary fibrosis???? in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/all-us-old-folks-with-radiation-induced-pulmonary-fibrosis/#post-32990</link>
				<pubDate>Wed, 31 Aug 2022 17:15:01 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/all-us-old-folks-with-radiation-induced-pulmonary-fibrosis/#post-32990"><span class="bb-reply-lable">Reply to</span> all us old folks with radiation induced pulmonary fibrosis????</a></p> <div class="bb-content-inr-wrap"><p>Just like IPF where some people last a couple of years and others are still around nearly 20 years after diagnosis, RIPF has varied outcomes and is rarer so there is much less data.  Anna has good information that I have also seen in scientific papers (all that chemistry and physics I studied in college has come in handy.) There is no cure&hellip;<span class="activity-read-more" id="activity-read-more-34969"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/all-us-old-folks-with-radiation-induced-pulmonary-fibrosis/#post-32990" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion all us old folks with radiation induced pulmonary fibrosis???? in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/all-us-old-folks-with-radiation-induced-pulmonary-fibrosis/#post-32972</link>
				<pubDate>Wed, 31 Aug 2022 04:05:49 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/all-us-old-folks-with-radiation-induced-pulmonary-fibrosis/#post-32972"><span class="bb-reply-lable">Reply to</span> all us old folks with radiation induced pulmonary fibrosis????</a></p> <div class="bb-content-inr-wrap"><p>Hello all,</p>
<p>I was diagnosed with radiation induced PF in January of this year six months after completing radiation for breast cancer (no chemo.)  The pattern of fibrosis is different from that of IPF: linear and reticular (net-like) rather than honeycombing. Prednisone is the standard first-line treatment. Ofev (not Esbriet) has been&hellip;<span class="activity-read-more" id="activity-read-more-34951"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/all-us-old-folks-with-radiation-induced-pulmonary-fibrosis/#post-32972" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion What is your experience with Curcumin? in the forum PF Life: 50+</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/what-is-your-experience-with-curcumin/#post-32928</link>
				<pubDate>Mon, 22 Aug 2022 13:10:40 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/what-is-your-experience-with-curcumin/#post-32928"><span class="bb-reply-lable">Reply to</span> What is your experience with Curcumin?</a></p> <div class="bb-content-inr-wrap"><p>Hi Natalie,</p>
<p>Curcumin is known for being an anti-inflammatory compound and is in turmeric which is used in Indian cooking and medicine.  The problem with it and supplements which contain it is its lack of bioavailability, even when combined with piperine (in black pepper) which helps absorption.  I have seen the promising research studies, but&hellip;<span class="activity-read-more" id="activity-read-more-34870"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/what-is-your-experience-with-curcumin/#post-32928" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Hyperbaric oxygen therapy in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/hyperbaric-oxygen-therapy/#post-32832</link>
				<pubDate>Thu, 04 Aug 2022 16:04:43 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/hyperbaric-oxygen-therapy/#post-32832"><span class="bb-reply-lable">Reply to</span> Hyperbaric oxygen therapy</a></p> <div class="bb-content-inr-wrap"><p>Hi Natalie,</p>
<p>Maybe you could get hyperbaric oxygen therapy for your edema and it would have the good side effect of helping your lungs.  I asked my pulmonologist (who only treats ILD at a large research hospital) if they would ever follow up on hyperbaric oxygen for radiation induced PF in human clinical trials.  He told me it was very unlikely&hellip;<span class="activity-read-more" id="activity-read-more-34689"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/hyperbaric-oxygen-therapy/#post-32832" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Hyperbaric oxygen therapy in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/hyperbaric-oxygen-therapy/#post-32830</link>
				<pubDate>Thu, 04 Aug 2022 03:17:57 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/hyperbaric-oxygen-therapy/#post-32830"><span class="bb-reply-lable">Reply to</span> Hyperbaric oxygen therapy</a></p> <div class="bb-content-inr-wrap"><p>Hi Natalie,</p>
<p>I know that hyperbaric oxygen therapy can help with radiation induced fibrosis in tissue and bone (such as in breast tissue necrosis or head and neck cancer) but have never heard of it being used to treat pulmonary fibrosis in humans.  I have PF from radiation for breast cancer but my breast tissue was not affected.  Studies have&hellip;<span class="activity-read-more" id="activity-read-more-34686"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/hyperbaric-oxygen-therapy/#post-32830" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Why do IPF patients lose weight and how to help in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/why-do-ipf-patients-lose-weight-and-how-to-help/#post-32642</link>
				<pubDate>Sat, 16 Jul 2022 11:21:05 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/why-do-ipf-patients-lose-weight-and-how-to-help/#post-32642"><span class="bb-reply-lable">Reply to</span> Why do IPF patients lose weight and how to help</a></p> <div class="bb-content-inr-wrap"><p>I take alendronate once a week for osteoporosis. I’m careful to drink lots of water with it and wait before eating to avoid esophagitis. I haven’t had any jawbone problems but I take good care of my teeth.  My doctor has me take a year off every few years to try to avoid the bad side effects and so far it has worked.                          &hellip;<span class="activity-read-more" id="activity-read-more-34379"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/why-do-ipf-patients-lose-weight-and-how-to-help/#post-32642" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Sleeping with head elevated in the forum Diagnosis​ ​Information​ ​and​ ​General​ ​Questions</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/sleeping-with-head-elevated/#post-32640</link>
				<pubDate>Fri, 15 Jul 2022 22:10:08 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/sleeping-with-head-elevated/#post-32640"><span class="bb-reply-lable">Reply to</span> Sleeping with head elevated</a></p> <div class="bb-content-inr-wrap"><p>I sleep with a wedge pillow and am fairly good about sticking to the suggested diet, omeprazole and anti-GERD protocols.  Four years ago I was hospitalized with a severe upper GI bleed.  I have never had any GERD symptoms but was diagnosed with esophagitis and Barrett&#8217;s esophagus.  I stuck to the recommendations of &#8220;The Acid Watcher Diet&#8221; by&hellip;<span class="activity-read-more" id="activity-read-more-34375"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/sleeping-with-head-elevated/#post-32640" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Bridging the Emotional Gap Between Patients and Doctors in the forum Welcome Lounge</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/bridging-the-emotional-gap-between-patients-and-doctors/#post-31788</link>
				<pubDate>Mon, 25 Apr 2022 19:08:35 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/bridging-the-emotional-gap-between-patients-and-doctors/#post-31788"><span class="bb-reply-lable">Reply to</span> Bridging the Emotional Gap Between Patients and Doctors</a></p> <div class="bb-content-inr-wrap"><p>I was sent to the ILD clinic at the hospital by my radiation oncologist after my post radiotherapy pneumonitis showed up on a chest CT as pulmonary fibrosis.  It was a bit of a shock having to turn my mind from worrying about stage 2 breast cancer (with an 85% five year survival rate) to something worse.  My pulmonologist answered my questions&hellip;<span class="activity-read-more" id="activity-read-more-32894"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/bridging-the-emotional-gap-between-patients-and-doctors/#post-31788" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret replied to the discussion Biopsy… yes or no? in the forum Upcoming Medical Appointments: Q&#38;As</title>
				<link>https://pulmonaryfibrosisnews.com/forums/forums/topic/biopsy-yes-or-no/#post-31593</link>
				<pubDate>Mon, 04 Apr 2022 03:17:13 -0500</pubDate>

									<content:encoded><![CDATA[<p class = "activity-discussion-title-wrap"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/biopsy-yes-or-no/#post-31593"><span class="bb-reply-lable">Reply to</span> Biopsy… yes or no?</a></p> <div class="bb-content-inr-wrap"><p>I have been recently diagnosed with radiation induced pulmonary fibrosis after breast cancer treatment (on HRCT) which is a rare side effect. My pulmonologist was not very surprised as I had an upper GI bleed and was diagnosed with Barrett’s esophagus four years ago. I have never had any symptoms of heartburn, but started taking omeprazole then.&hellip;<span class="activity-read-more" id="activity-read-more-32544"><a href="https://pulmonaryfibrosisnews.com/forums/forums/topic/biopsy-yes-or-no/#post-31593" rel="nofollow"> Read more</a></span></p>
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				<title>Margaret posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/31551/#acomment-31614</link>
				<pubDate>Tue, 15 Feb 2022 07:34:52 -0600</pubDate>

									<content:encoded><![CDATA[<p>Thank you for the links.</p>
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					<a href="https://pulmonaryfibrosisnews.com/forums/members/msherbert/" data-bb-hp-profile="13012" rel="nofollow">Margaret</a> became a registered member					]]></content:encoded>
				
				
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				<title>Margaret posted a new activity comment</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/31551/#acomment-31594</link>
				<pubDate>Sun, 13 Feb 2022 16:06:39 -0600</pubDate>

									<content:encoded><![CDATA[<p>Thanks, Charlene.  I don&#8217;t have IPF like most people here since my PF is an adverse effect of radiation treatment for breast cancer. Even my pulmonologist who heads the ILD program at a large research hospital doesn&#8217;t have much experience with this to go on since most RILI patients he has treated developed PF after radiation for lung cancer.&hellip;<span class="activity-read-more" id="activity-read-more-31594"><a href="https://pulmonaryfibrosisnews.com/forums/activity/p/31551/#acomment-31594" rel="nofollow"> Read more</a></span></p>
				<strong>In reply to</strong> -
					<a href="https://pulmonaryfibrosisnews.com/forums/members/msherbert/" data-bb-hp-profile="13012" rel="nofollow">Margaret</a> became a registered member					]]></content:encoded>
				
				
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				<title>Margaret became a registered member</title>
				<link>https://pulmonaryfibrosisnews.com/forums/activity/p/31551/</link>
				<pubDate>Wed, 09 Feb 2022 15:53:55 -0600</pubDate>

				
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